NDC 63323-012 – Oxytocin

Oxytocin 10 [USP'U]/mL · Injection, Solution · Intramuscular, Intravenous

Human Prescription Drug 1 recall

Product NDC63323-012

Product details

Brand name
Oxytocin
Generic name
Oxytocin
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Marketing category
NDA · NDA018248
Marketed since
August 10, 2000
Listing expires
December 31, 2027
Pharmacologic class
Oxytocic

Active ingredients

Uses, dosage, side effects and warnings for Oxytocin →

Package NDC codes (4)

Package NDCDescriptionSince
63323-012-0725 VIAL in 1 TRAY (63323-012-07) / 1 mL in 1 VIAL (63323-012-17)Aug 10, 2000
63323-012-1025 VIAL, MULTI-DOSE in 1 TRAY (63323-012-10) / 10 mL in 1 VIAL, MULTI-DOSE (63323-012-06)Aug 10, 2000
63323-012-1125 VIAL in 1 TRAY (63323-012-11) / 1 mL in 1 VIAL (63323-012-03)Aug 10, 2000
63323-012-3010 VIAL, MULTI-DOSE in 1 TRAY (63323-012-30) / 30 mL in 1 VIAL, MULTI-DOSE (63323-012-02)Aug 10, 2000

Recalls mentioning this NDC

Other Oxytocin products